Division of Endocrinology and Metabolism, Department of Internal Medicine, Universidad del Cauca, Popayan, Colombia.
Centro de Investigación Arequipa - EXACTA LAB SAC, Yanahuara, Peru.
Diabetes Obes Metab. 2023 Jan;25(1):238-247. doi: 10.1111/dom.14868. Epub 2022 Oct 9.
To evaluate the real-world effectiveness and safety of insulin glargine 300 U/ml (Gla-300) in achieving glycaemic goals in insulin-naïve people with type 2 diabetes (T2D) in Mexico, Colombia and Peru (Latin America region) in the A Toujeo Observational Study (ATOS).
ATOS was a multicentre, prospective, 12-month observational study, which included 4422 insulin-naïve adults (age ≥ 18 years) with T2D uncontrolled (HbA1c > 7% and ≤11%) on at least one oral antidiabetic drug (OAD) who initiated Gla-300 treatment as per routine practice. The primary endpoint was the percentage of participants achieving their predefined individualized HbA1c goal at month 6. Key secondary endpoints included change from baseline in HbA1c, fasting plasma glucose (FPG), fasting self-monitored blood glucose (SMBG), body weight and incidence of hypoglycaemia.
In this subgroup analysis, a total of 314 participants with T2D received Gla-300. At baseline, mean ± SD age was 56.0 ± 11.6 years, duration of diabetes was 9.7 ± 6.6 years and 65.9% of participants were on at least two OADs. The individualized HbA1c target was achieved by 25.8% of participants (95% confidence interval [CI]: 20.3-31.9) at month 6 and by 35.3% (95% CI: 28.5-42.5) at month 12. Gla-300 treatment improved glycaemic control with meaningful reductions in mean HbA1c, FPG and fasting SMBG. The incidence of hypoglycaemia reported was low and body weight remained stable.
In a real-world setting in the Latin America region, the initiation of Gla-300 in people with T2D uncontrolled on OADs resulted in improved glycaemic control with a low incidence of hypoglycaemia and no change in body weight.
评估甘精胰岛素 300U/ml(Gla-300)在墨西哥、哥伦比亚和秘鲁(拉丁美洲地区)未经胰岛素治疗的 2 型糖尿病(T2D)人群中达到血糖目标的真实疗效和安全性,该项研究来自 A Toujeo 观察性研究(ATOS)。
ATOS 是一项多中心、前瞻性、12 个月观察性研究,纳入了 4422 例年龄≥18 岁、正在接受至少一种口服降糖药(OAD)治疗且血糖控制不佳(HbA1c>7%且≤11%)的 T2D 初治患者。这些患者按照常规治疗方案起始甘精胰岛素 300U/ml 治疗。主要终点是第 6 个月时达到个体化 HbA1c 目标的患者比例。次要终点包括基线时 HbA1c、空腹血糖(FPG)、空腹自我监测血糖(SMBG)、体重和低血糖发生率的变化。
在这项亚组分析中,共有 314 例 T2D 患者接受了甘精胰岛素 300U/ml 治疗。基线时,患者的平均年龄±标准差为 56.0±11.6 岁,糖尿病病程为 9.7±6.6 年,65.9%的患者正在服用至少两种 OAD。第 6 个月时,25.8%(95%置信区间[CI]:20.3-31.9)的患者达到个体化 HbA1c 目标,第 12 个月时,35.3%(95% CI:28.5-42.5)的患者达到目标。甘精胰岛素 300U/ml 治疗改善了血糖控制,HbA1c、FPG 和空腹 SMBG 均显著降低。低血糖报告发生率较低,体重保持稳定。
在拉丁美洲地区的真实环境中,在 OAD 治疗血糖控制不佳的 T2D 患者中起始甘精胰岛素 300U/ml 治疗可改善血糖控制,低血糖发生率低,体重无变化。